- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01751464
A WrapAround Case Management Program for Youth Injured by Violence
July 4, 2013 updated by: Dr. Carolyn Snider, University of Manitoba
A WrapAround Case Management Program for Youth Injured by Violence: A Feasibility Study
This is a feasibility study of a WrapAround Case Management Program for Youth Injured by Violence.
Youth (aged 10-24) who have been injured by violence and visit the emergency department will be offered a support worker who will provide WrapAround Case Management.
This study is designed to assess the feasibility of recruitment, enrollment and follow-up.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
8
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Manitoba
-
Winnipeg, Manitoba, Canada, R3P 3E4
- Winnipeg Health Sciences Centre
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
10 years to 24 years (Child, Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Age 10 - 24 and
- Presentation to an ED or trauma floor with an injury caused by violence (defined as an injury inflicted by someone else and one of a gunshot wound, stab wound, injury due to blunt object, or injury due to bodily force).
Exclusion Criteria:
- Unable to consent due to language or brain injury,
- Sexual assault,
- Child Abuse
- Self-Inflicted Injury,
- Subject is under arrest or
- Non-resident of Winnipeg.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: WrapAround Care
|
Youth Injured by Violence will be paired with a support worker who has extensive experience working with youth affected by violence.It is important to note that the wraparound concept involves individualized care planning and management.
As such, the specific care plan will be different for each participant.
Through early intensive meetings, they will develop a mentoring relationship.
They will work with the youth to develop a support team, which may include family, teachers, child welfare workers and truly anyone the youth has decided can help them in their path to making positive choices.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
To estimate the recruitment rate of an ED referral program for injured youth
Time Frame: 6 months
|
We will evaluate the proportion of eligible patients who are identified for enrolment and any biases in subject identification
|
6 months
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
To identify barriers to participation in a hospital-based case management program
Time Frame: 6 months
|
6 months
|
|
To determine the average number of contacts and amount of time required per participant
Time Frame: 6 months
|
6 months
|
|
To estimate the rates of follow-up among those successfully recruited
Time Frame: 6 months
|
6 months
|
|
To determine the most appropriate way to notify the case manager of an eligible participant
Time Frame: 6 months
|
6 months
|
|
To determine the most successful enrollment strategy for retention of participants
Time Frame: 6 months
|
6 months
|
|
To determine level of engagement between the case manager and youth
Time Frame: 6 months
|
6 months
|
|
To determine the most appropriate method of follow-up
Time Frame: 6 months
|
6 months
|
|
To determine the impact in violence-related attitudes and behaviours among participants
Time Frame: 6 months
|
6 months
|
|
To determine the impact on recurrent intentional injury amongst participants
Time Frame: 6 months
|
6 months
|
|
To determine the impact on modifiable risk factors
Time Frame: 6 months
|
6 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Carolyn E Snider, MD MPH, University of Manitoba
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
November 1, 2012
Primary Completion (Actual)
June 1, 2013
Study Completion (Actual)
June 1, 2013
Study Registration Dates
First Submitted
December 13, 2012
First Submitted That Met QC Criteria
December 13, 2012
First Posted (Estimate)
December 18, 2012
Study Record Updates
Last Update Posted (Estimate)
July 8, 2013
Last Update Submitted That Met QC Criteria
July 4, 2013
Last Verified
July 1, 2013
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- H2012:133
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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